All Photos(1)
About This Item
Linear Formula:
BrC6H2(OCH3)2CHO
CAS Number:
Molecular Weight:
245.07
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
97%
mp
81-84 °C (lit.)
functional group
aldehyde
bromo
SMILES string
COc1cc(Br)cc(C=O)c1OC
InChI
1S/C9H9BrO3/c1-12-8-4-7(10)3-6(5-11)9(8)13-2/h3-5H,1-2H3
InChI key
RVMWFOFQRYTRHZ-UHFFFAOYSA-N
General description
5-Bromo-2,3-dimethoxybenzaldehyde can be prepared by employing 5-bromo-2-hydroxy-3-methoxybenzaldehyde as a starting reagent.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
The cyclisation of benzylaminonitriles. Part 7. Regiospecific formation of methoxy-substituted isoquinolin-4-ones using methylthio activating groups.
Gavin JP and Waigh RD.
Journal of the Chemical Society. Perkin Transactions 1, 3, 503-508 (1990)
Flavonoids syntheses. V. Synthesis of flavonoids with three hydroxy and four methoxy groups and their spectral properties.
Iinuma M, et al.
Chemical & Pharmaceutical Bulletin, 35(2), 660-667 (1987)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service